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Updated: Sep 16, 2026

Preparation of 3D Collagen Gels and Microchannels for the Study of 3D Interactions In Vivo
Published on: May 9, 2016
Rapid Fabrication of Capillary-Sized Microchannels in Collagen Hydrogel via Thermally Responsive Gelatin Microfiber
Takayuki Takei1, Momoka Nakamura1, Ko Nishimura1
1Department of Chemical Engineering, Graduate School of Science and Engineering, Kagoshima University, 1-21-40 Korimoto, Kagoshima 890-0065, Japan.
Abstract:
Engineering volumetric three-dimensional tissues requires the rapid establishment of dense, capillary-like microchannels to ensure adequate oxygen and nutrient supply while preventing hypoxic cell necrosis. Sacrificial microfiber templating approaches using lower critical solution temperature (LCST) polymers cannot employ type I collagen hydrogels-a biologically ideal extracellular matrix-because LCST fiber dissolution in cold collagen solutions precedes matrix gelation owing to thermodynamic mismatch. Here, we present a proof-of-concept strategy to rapidly fabricate capillary-sized microchannels within collagen hydrogels using thermoresponsive, physically crosslinked gelatin microfibers as sacrificial templates. Three-dimensional gelatin microfibers with capillary-sized diameters (approximately 10 μm) were fabricated via wet spinning and embedded in a type I collagen aqueous solution (4 °C). Open microchannels throughout the collagen matrix were successfully generated within 1 h of sequential thermal incubation (20 °C for collagen gelation and subsequently 37 °C for gelatin thermal dissolution), without cytotoxic chemicals. Active particle flow confirmed channel patency and fluidic continuity. Additionally, heparinized rat blood readily perfused through the channels, and scanning electron microscopy revealed open microchannel cross-sections (diameter: approximately 10 μm). This simple, thermally controlled approach resolves the limited temperature compatibility between collagen matrices and sacrificial microfibers, serving as a promising biofabrication foundation for engineering tissue constructs.

